These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

226 related items for PubMed ID: 24506995

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. [Characterization of two Chinese families with aminoglycoside-induced and nonsyndromic hearing loss both carrying a mitochondrial 12S rRNA 1494C>T mutation].
    Gong SS, Chen BB, Peng GH, Zheng J, Zhang T, Zheng BJ, Fang F, Zhang CQ, Lv JX, Guan MX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Aug; 29(4):382-7. PubMed ID: 22875491
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. The mitochondrial transfer RNAAsp A7551G mutation may contribute to the clinical expression of deafness associated with the A1555G mutation in a pedigree with hearing impairment.
    Zhang J, Lu B, Xia WW, Fang B, Ding XX, Hu GW.
    Mol Med Rep; 2019 Mar; 19(3):1797-1802. PubMed ID: 30592262
    [Abstract] [Full Text] [Related]

  • 5. Very low penetrance of hearing loss in seven Han Chinese pedigrees carrying the deafness-associated 12S rRNA A1555G mutation.
    Tang X, Yang L, Zhu Y, Liao Z, Wang J, Qian Y, Tao Z, Hu L, Wu G, Lan J, Wang X, Ji J, Wu J, Ji Y, Feng J, Chen J, Li Z, Zhang X, Lu J, Guan MX.
    Gene; 2007 May 15; 393(1-2):11-9. PubMed ID: 17341440
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Maternally inherited hearing loss is associated with the novel mitochondrial tRNA Ser(UCN) 7505T>C mutation in a Han Chinese family.
    Tang X, Li R, Zheng J, Cai Q, Zhang T, Gong S, Zheng W, He X, Zhu Y, Xue L, Yang A, Yang L, Lu J, Guan MX.
    Mol Genet Metab; 2010 May 15; 100(1):57-64. PubMed ID: 20153673
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. [Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss in five Han Chinese pedigrees].
    Zhang T, Chen BB, Zheng J, Gong SS, Zhang CQ, Lv JX, Guan MX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Aug 15; 28(4):367-73. PubMed ID: 21811972
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. [Hearing loss and epilepsy may be associated with the novel mitochondrial tRNASer(UCN) 7472delC mutation in a Chinese family].
    Zhao JY, Tang XW, Lan JS, Lv JX, Yang L, Li ZY, Zhu Y, Sun DM, Yang AF, Wang JD, Xu J, Guan MX.
    Yi Chuan; 2008 Dec 15; 30(12):1557-62. PubMed ID: 19073569
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. The Mitochondrial tRNAHis G12192A Mutation May Modulate the Clinical Expression of Deafness-Associated tRNAThr G15927A Mutation in a Chinese Pedigree.
    Ding Y, Teng YS, Zhuo GC, Xia BH, Leng JH.
    Curr Mol Med; 2019 Dec 15; 19(2):136-146. PubMed ID: 30854964
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Mitochondrial COX2 G7598A mutation may have a modifying role in the phenotypic manifestation of aminoglycoside antibiotic-induced deafness associated with 12S rRNA A1555G mutation in a Han Chinese pedigree.
    Chen T, Liu Q, Jiang L, Liu C, Ou Q.
    Genet Test Mol Biomarkers; 2013 Feb 15; 17(2):122-30. PubMed ID: 23256547
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. [Mutation analysis of mitochondrial 12S rRNA gene G709A in a maternally inherited pedigree with non-syndromic deafness].
    Wei Q, Lu Y, Zhang Y, Chen Z, Xing G, Cao X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec 15; 26(6):610-4. PubMed ID: 19953480
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 12.